Canonical Allele Identifier: PA2827990783
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411444
ClinVar RCV Id: RCV000479660 RCV000571928 RCV001192982 RCV002506131 RCV003766575 RCV004001947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg12His
CA030877
NM_001354901.2:c.35G>A